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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs199705686

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chrY:57189539 (GRCh38.p14) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

This SNP has mapping conflicts. See here for details.

Alleles
G>A / G>C
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.000008 (2/251136, GnomAD_exome)
C=0.000008 (1/121378, ExAC)
C=0.0002 (1/4805, 1000G_30x) (+ 1 more)
A=0.0004 (2/4470, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
IL9R : Missense Variant
Publications
0 citations
Genomic View
See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 4470 G=0.9996 A=0.0004
European Sub 4462 G=0.9996 A=0.0004
African Sub 0 G=0 A=0
African Others Sub 0 G=0 A=0
African American Sub 0 G=0 A=0
Asian Sub 0 G=0 A=0
East Asian Sub 0 G=0 A=0
Other Asian Sub 0 G=0 A=0
Latin American 1 Sub 0 G=0 A=0
Latin American 2 Sub 0 G=0 A=0
South Asian Sub 0 G=0 A=0
Other Sub 8 G=1.0 A=0.0


Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
gnomAD - Exomes Global Study-wide 251136 G=0.999992 C=0.000008
gnomAD - Exomes European Sub 135084 G=1.000000 C=0.000000
gnomAD - Exomes Asian Sub 49008 G=0.99996 C=0.00004
gnomAD - Exomes American Sub 34584 G=1.00000 C=0.00000
gnomAD - Exomes African Sub 16254 G=1.00000 C=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 10076 G=1.00000 C=0.00000
gnomAD - Exomes Other Sub 6130 G=1.0000 C=0.0000
ExAC Global Study-wide 121378 G=0.999992 C=0.000008
ExAC Europe Sub 73336 G=1.00000 C=0.00000
ExAC Asian Sub 25164 G=0.99996 C=0.00004
ExAC American Sub 11570 G=1.00000 C=0.00000
ExAC African Sub 10400 G=1.00000 C=0.00000
ExAC Other Sub 908 G=1.000 C=0.000
1000Genomes_30x Global Study-wide 4805 G=0.9998 C=0.0002
1000Genomes_30x African Sub 1328 G=1.0000 C=0.0000
1000Genomes_30x Europe Sub 961 G=1.000 C=0.000
1000Genomes_30x South Asian Sub 883 G=1.000 C=0.000
1000Genomes_30x East Asian Sub 878 G=0.999 C=0.001
1000Genomes_30x American Sub 755 G=1.000 C=0.000
Allele Frequency Aggregator Total Global 4470 G=0.9996 A=0.0004
Allele Frequency Aggregator European Sub 4462 G=0.9996 A=0.0004
Allele Frequency Aggregator Other Sub 8 G=1.0 A=0.0
Allele Frequency Aggregator Latin American 1 Sub 0 G=0 A=0
Allele Frequency Aggregator Latin American 2 Sub 0 G=0 A=0
Allele Frequency Aggregator South Asian Sub 0 G=0 A=0
Allele Frequency Aggregator African Sub 0 G=0 A=0
Allele Frequency Aggregator Asian Sub 0 G=0 A=0
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p14 chr Y NC_000024.10:g.57189539G>A
GRCh38.p14 chr Y NC_000024.10:g.57189539G>C
GRCh37.p13 chr Y NC_000024.9:g.59335690G>A
GRCh37.p13 chr Y NC_000024.9:g.59335690G>C
IL9R RefSeqGene NG_013238.1:g.10439G>A
IL9R RefSeqGene NG_013238.1:g.10439G>C
GRCh38.p14 chr X NC_000023.11:g.156003019G>A
GRCh38.p14 chr X NC_000023.11:g.156003019G>C
GRCh37.p13 chr X NC_000023.10:g.155232684G>A
GRCh37.p13 chr X NC_000023.10:g.155232684G>C
Gene: IL9R, interleukin 9 receptor (plus strand)
Molecule type Change Amino acid[Codon] SO Term
IL9R transcript variant 1 NM_002186.3:c.142G>A G [GGG] > R [AGG] Coding Sequence Variant
interleukin-9 receptor isoform 1 precursor NP_002177.2:p.Gly48Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant 1 NM_002186.3:c.142G>C G [GGG] > R [CGG] Coding Sequence Variant
interleukin-9 receptor isoform 1 precursor NP_002177.2:p.Gly48Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant 2 NM_176786.2:c.283G>A G [GGG] > R [AGG] Coding Sequence Variant
interleukin-9 receptor isoform 2 NP_789743.2:p.Gly95Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant 2 NM_176786.2:c.283G>C G [GGG] > R [CGG] Coding Sequence Variant
interleukin-9 receptor isoform 2 NP_789743.2:p.Gly95Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X8 XM_017029502.2:c.29-1401G…

XM_017029502.2:c.29-1401G>A

 		N/A Intron Variant
IL9R transcript variant X11 XM_017029506.2:c. N/A Genic Upstream Transcript Variant
IL9R transcript variant X1 XM_011531151.3:c.283G>A G [GGG] > R [AGG] Coding Sequence Variant
interleukin-9 receptor isoform X1 XP_011529453.1:p.Gly95Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X1 XM_011531151.3:c.283G>C G [GGG] > R [CGG] Coding Sequence Variant
interleukin-9 receptor isoform X1 XP_011529453.1:p.Gly95Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X2 XM_017029495.2:c.283G>A G [GGG] > R [AGG] Coding Sequence Variant
interleukin-9 receptor isoform X2 XP_016884984.1:p.Gly95Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X2 XM_017029495.2:c.283G>C G [GGG] > R [CGG] Coding Sequence Variant
interleukin-9 receptor isoform X2 XP_016884984.1:p.Gly95Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X3 XM_011531152.3:c.259G>A G [GGG] > R [AGG] Coding Sequence Variant
interleukin-9 receptor isoform X3 XP_011529454.1:p.Gly87Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X3 XM_011531152.3:c.259G>C G [GGG] > R [CGG] Coding Sequence Variant
interleukin-9 receptor isoform X3 XP_011529454.1:p.Gly87Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X4 XM_047442092.1:c.151G>A G [GGG] > R [AGG] Coding Sequence Variant
interleukin-9 receptor isoform X4 XP_047298048.1:p.Gly51Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X4 XM_047442092.1:c.151G>C G [GGG] > R [CGG] Coding Sequence Variant
interleukin-9 receptor isoform X4 XP_047298048.1:p.Gly51Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X5 XM_011531155.3:c.283G>A G [GGG] > R [AGG] Coding Sequence Variant
interleukin-9 receptor isoform X5 XP_011529457.1:p.Gly95Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X5 XM_011531155.3:c.283G>C G [GGG] > R [CGG] Coding Sequence Variant
interleukin-9 receptor isoform X5 XP_011529457.1:p.Gly95Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X6 XM_047442093.1:c.283G>A G [GGG] > R [AGG] Coding Sequence Variant
interleukin-9 receptor isoform X6 XP_047298049.1:p.Gly95Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X6 XM_047442093.1:c.283G>C G [GGG] > R [CGG] Coding Sequence Variant
interleukin-9 receptor isoform X6 XP_047298049.1:p.Gly95Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X7 XM_047442094.1:c.259G>A G [GGG] > R [AGG] Coding Sequence Variant
interleukin-9 receptor isoform X7 XP_047298050.1:p.Gly87Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X7 XM_047442094.1:c.259G>C G [GGG] > R [CGG] Coding Sequence Variant
interleukin-9 receptor isoform X7 XP_047298050.1:p.Gly87Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X9 XM_011531157.3:c.283G>A G [GGG] > R [AGG] Coding Sequence Variant
interleukin-9 receptor isoform X9 XP_011529459.1:p.Gly95Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X9 XM_011531157.3:c.283G>C G [GGG] > R [CGG] Coding Sequence Variant
interleukin-9 receptor isoform X9 XP_011529459.1:p.Gly95Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X10 XM_047442095.1:c.259G>A G [GGG] > R [AGG] Coding Sequence Variant
interleukin-9 receptor isoform X10 XP_047298051.1:p.Gly87Arg G (Gly) > R (Arg) Missense Variant
IL9R transcript variant X10 XM_047442095.1:c.259G>C G [GGG] > R [CGG] Coding Sequence Variant
interleukin-9 receptor isoform X10 XP_047298051.1:p.Gly87Arg G (Gly) > R (Arg) Missense Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement G= A C
GRCh38.p14 chr Y NC_000024.10:g.57189539= NC_000024.10:g.57189539G>A NC_000024.10:g.57189539G>C
GRCh37.p13 chr Y NC_000024.9:g.59335690= NC_000024.9:g.59335690G>A NC_000024.9:g.59335690G>C
IL9R RefSeqGene NG_013238.1:g.10439= NG_013238.1:g.10439G>A NG_013238.1:g.10439G>C
IL9R transcript variant 1 NM_002186.3:c.142= NM_002186.3:c.142G>A NM_002186.3:c.142G>C
IL9R transcript variant 1 NM_002186.2:c.142= NM_002186.2:c.142G>A NM_002186.2:c.142G>C
IL9R transcript variant 2 NM_176786.2:c.283= NM_176786.2:c.283G>A NM_176786.2:c.283G>C
IL9R transcript variant 2 NM_176786.1:c.283= NM_176786.1:c.283G>A NM_176786.1:c.283G>C
GRCh38.p14 chr X NC_000023.11:g.156003019= NC_000023.11:g.156003019G>A NC_000023.11:g.156003019G>C
GRCh37.p13 chr X NC_000023.10:g.155232684= NC_000023.10:g.155232684G>A NC_000023.10:g.155232684G>C
IL9R transcript variant X5 XM_011531155.3:c.283= XM_011531155.3:c.283G>A XM_011531155.3:c.283G>C
IL9R transcript variant X10 XM_011531155.2:c.283= XM_011531155.2:c.283G>A XM_011531155.2:c.283G>C
IL9R transcript variant X5 XM_011531155.1:c.283= XM_011531155.1:c.283G>A XM_011531155.1:c.283G>C
IL9R transcript variant X1 XM_011531151.3:c.283= XM_011531151.3:c.283G>A XM_011531151.3:c.283G>C
IL9R transcript variant X1 XM_011531151.2:c.283= XM_011531151.2:c.283G>A XM_011531151.2:c.283G>C
IL9R transcript variant X1 XM_011531151.1:c.283= XM_011531151.1:c.283G>A XM_011531151.1:c.283G>C
IL9R transcript variant X3 XM_011531152.3:c.259= XM_011531152.3:c.259G>A XM_011531152.3:c.259G>C
IL9R transcript variant X3 XM_011531152.2:c.259= XM_011531152.2:c.259G>A XM_011531152.2:c.259G>C
IL9R transcript variant X2 XM_011531152.1:c.259= XM_011531152.1:c.259G>A XM_011531152.1:c.259G>C
IL9R transcript variant X9 XM_011531157.3:c.283= XM_011531157.3:c.283G>A XM_011531157.3:c.283G>C
IL9R transcript variant X17 XM_011531157.2:c.283= XM_011531157.2:c.283G>A XM_011531157.2:c.283G>C
IL9R transcript variant X7 XM_011531157.1:c.283= XM_011531157.1:c.283G>A XM_011531157.1:c.283G>C
IL9R transcript variant X5 XM_011545650.3:c.283= XM_011545650.3:c.283G>A XM_011545650.3:c.283G>C
IL9R transcript variant X10 XM_011545650.2:c.283= XM_011545650.2:c.283G>A XM_011545650.2:c.283G>C
IL9R transcript variant X5 XM_011545650.1:c.283= XM_011545650.1:c.283G>A XM_011545650.1:c.283G>C
IL9R transcript variant X3 XM_011545646.3:c.259= XM_011545646.3:c.259G>A XM_011545646.3:c.259G>C
IL9R transcript variant X3 XM_011545646.2:c.259= XM_011545646.2:c.259G>A XM_011545646.2:c.259G>C
IL9R transcript variant X2 XM_011545646.1:c.259= XM_011545646.1:c.259G>A XM_011545646.1:c.259G>C
IL9R transcript variant X9 XM_011545652.3:c.283= XM_011545652.3:c.283G>A XM_011545652.3:c.283G>C
IL9R transcript variant X17 XM_011545652.2:c.283= XM_011545652.2:c.283G>A XM_011545652.2:c.283G>C
IL9R transcript variant X7 XM_011545652.1:c.283= XM_011545652.1:c.283G>A XM_011545652.1:c.283G>C
IL9R transcript variant X2 XM_017029495.2:c.283= XM_017029495.2:c.283G>A XM_017029495.2:c.283G>C
IL9R transcript variant X2 XM_017029495.1:c.283= XM_017029495.1:c.283G>A XM_017029495.1:c.283G>C
IL9R transcript variant X1 XM_011545645.3:c.283= XM_011545645.3:c.283G>A XM_011545645.3:c.283G>C
IL9R transcript variant X1 XM_011545645.2:c.283= XM_011545645.2:c.283G>A XM_011545645.2:c.283G>C
IL9R transcript variant X1 XM_011545645.1:c.283= XM_011545645.1:c.283G>A XM_011545645.1:c.283G>C
IL9R transcript variant X2 XM_017030044.2:c.283= XM_017030044.2:c.283G>A XM_017030044.2:c.283G>C
IL9R transcript variant X2 XM_017030044.1:c.283= XM_017030044.1:c.283G>A XM_017030044.1:c.283G>C
IL9R transcript variant X7 XM_047442094.1:c.259= XM_047442094.1:c.259G>A XM_047442094.1:c.259G>C
IL9R transcript variant X4 XM_047442092.1:c.151= XM_047442092.1:c.151G>A XM_047442092.1:c.151G>C
IL9R transcript variant X6 XM_047442093.1:c.283= XM_047442093.1:c.283G>A XM_047442093.1:c.283G>C
IL9R transcript variant 2 NR_024033.1:n.446= NR_024033.1:n.446G>A NR_024033.1:n.446G>C
IL9R transcript variant X10 XM_047442095.1:c.259= XM_047442095.1:c.259G>A XM_047442095.1:c.259G>C
IL9R transcript variant X7 XM_047442734.1:c.259= XM_047442734.1:c.259G>A XM_047442734.1:c.259G>C
IL9R transcript variant X4 XM_047442732.1:c.151= XM_047442732.1:c.151G>A XM_047442732.1:c.151G>C
IL9R transcript variant X6 XM_047442733.1:c.283= XM_047442733.1:c.283G>A XM_047442733.1:c.283G>C
IL9R transcript variant X10 XM_047442735.1:c.259= XM_047442735.1:c.259G>A XM_047442735.1:c.259G>C
interleukin-9 receptor isoform 1 precursor NP_002177.2:p.Gly48= NP_002177.2:p.Gly48Arg NP_002177.2:p.Gly48Arg
interleukin-9 receptor isoform 2 NP_789743.2:p.Gly95= NP_789743.2:p.Gly95Arg NP_789743.2:p.Gly95Arg
interleukin-9 receptor isoform X5 XP_011543952.1:p.Gly95= XP_011543952.1:p.Gly95Arg XP_011543952.1:p.Gly95Arg
interleukin-9 receptor isoform X3 XP_011543948.1:p.Gly87= XP_011543948.1:p.Gly87Arg XP_011543948.1:p.Gly87Arg
interleukin-9 receptor isoform X9 XP_011543954.1:p.Gly95= XP_011543954.1:p.Gly95Arg XP_011543954.1:p.Gly95Arg
interleukin-9 receptor isoform X1 XP_011543947.1:p.Gly95= XP_011543947.1:p.Gly95Arg XP_011543947.1:p.Gly95Arg
interleukin-9 receptor isoform X2 XP_016885533.1:p.Gly95= XP_016885533.1:p.Gly95Arg XP_016885533.1:p.Gly95Arg
interleukin-9 receptor isoform X7 XP_047298690.1:p.Gly87= XP_047298690.1:p.Gly87Arg XP_047298690.1:p.Gly87Arg
interleukin-9 receptor isoform X4 XP_047298688.1:p.Gly51= XP_047298688.1:p.Gly51Arg XP_047298688.1:p.Gly51Arg
interleukin-9 receptor isoform X6 XP_047298689.1:p.Gly95= XP_047298689.1:p.Gly95Arg XP_047298689.1:p.Gly95Arg
interleukin-9 receptor isoform X10 XP_047298691.1:p.Gly87= XP_047298691.1:p.Gly87Arg XP_047298691.1:p.Gly87Arg
IL9R transcript variant X8 XM_017029502.2:c.29-1401= XM_017029502.2:c.29-1401G>A XM_017029502.2:c.29-1401G>C
IL9R transcript variant X8 XM_017030051.2:c.29-1401= XM_017030051.2:c.29-1401G>A XM_017030051.2:c.29-1401G>C
interleukin-9 receptor isoform X1 XP_011529453.1:p.Gly95= XP_011529453.1:p.Gly95Arg XP_011529453.1:p.Gly95Arg
interleukin-9 receptor isoform X3 XP_011529454.1:p.Gly87= XP_011529454.1:p.Gly87Arg XP_011529454.1:p.Gly87Arg
interleukin-9 receptor isoform X5 XP_011529457.1:p.Gly95= XP_011529457.1:p.Gly95Arg XP_011529457.1:p.Gly95Arg
interleukin-9 receptor isoform X9 XP_011529459.1:p.Gly95= XP_011529459.1:p.Gly95Arg XP_011529459.1:p.Gly95Arg
interleukin-9 receptor isoform X2 XP_016884984.1:p.Gly95= XP_016884984.1:p.Gly95Arg XP_016884984.1:p.Gly95Arg
interleukin-9 receptor isoform X4 XP_047298048.1:p.Gly51= XP_047298048.1:p.Gly51Arg XP_047298048.1:p.Gly51Arg
interleukin-9 receptor isoform X6 XP_047298049.1:p.Gly95= XP_047298049.1:p.Gly95Arg XP_047298049.1:p.Gly95Arg
interleukin-9 receptor isoform X7 XP_047298050.1:p.Gly87= XP_047298050.1:p.Gly87Arg XP_047298050.1:p.Gly87Arg
interleukin-9 receptor isoform X10 XP_047298051.1:p.Gly87= XP_047298051.1:p.Gly87Arg XP_047298051.1:p.Gly87Arg
Help

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

6 SubSNP, 4 Frequency submissions
No Submitter Submission ID Date (Build)
1 1000GENOMES ss489235788 May 04, 2012 (137)
2 EVA_EXAC ss1694666492 Apr 01, 2015 (144)
3 GNOMAD ss2746167837 Nov 08, 2017 (151)
4 GNOMAD ss2984837589 Nov 08, 2017 (151)
5 1000G_HIGH_COVERAGE ss5623740896 Oct 13, 2022 (156)
6 EVA ss5897860334 Oct 13, 2022 (156)
7 1000Genomes_30x NC_000023.11 - 156003019 Oct 13, 2022 (156)
8 ExAC NC_000023.10 - 155232684 Oct 12, 2018 (152)
9 gnomAD - Exomes NC_000023.10 - 155232684 Jul 14, 2019 (153)
10 ALFA NC_000024.10 - 57189539 Apr 27, 2021 (155)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss2746167837, ss2984837589 NC_000023.10:155232683:G:A NC_000024.10:57189538:G:A (self)
15394285797 NC_000024.10:57189538:G:A NC_000024.10:57189538:G:A (self)
10178641, 14960268, ss489235788, ss1694666492 NC_000023.10:155232683:G:C NC_000024.10:57189538:G:C (self)
111266831, ss5623740896, ss5897860334 NC_000023.11:156003018:G:C NC_000024.10:57189538:G:C
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs199705686

Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
Top▲ Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post761+d5e8e07